首页> 外文期刊>The Permanente Journal >Use of ERC-1671 Vaccine in a Patient with Recurrent Glioblastoma Multiforme after Progression during Bevacizumab Therapy: First Published Report
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Use of ERC-1671 Vaccine in a Patient with Recurrent Glioblastoma Multiforme after Progression during Bevacizumab Therapy: First Published Report

机译:贝伐单抗治疗进展后复发性多形胶质母细胞瘤患者使用ERC-1671疫苗:首次发表的报告

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Objectives: Glioblastoma multiforme (GBM) is a highly aggressive tumor, which recurs despite resection, focal beam radiation, and temozolomide chemotherapy. At recurrence, the only second-line treatment approved by the US Food and Drug Administration is bevacizumab (Avastin). To date, no single agent has shown to extend the life of patients with progressive malignant gliomas after bevacizumab failure. Once the tumor recurs during bevacizumab therapy, it is universally fatal, with death occurring within a few weeks. ERC-1671 is an experimental treatment strategy, which uses the patient's own immune system to attack the tumor cells. We report preliminary data on the first human administration of ERC-1671 vaccination, under a single-patient, compassionate-use protocol, to a patient with progressive, bevacizumab-resistant GBM.Methods: Treatment involved sequential administration to the patient of GBM tumor cells and cell lysates combined from three different donors with GBM, followed by the patient's own tumor cells and lysates. Results: The patient survived for ten months after the vaccine administration without any other adjuvant therapy and died of complications related to his previous chemotherapies. The tissues collected after two vaccination cycles and at the time of death showed a robust immune response and no viable tumor. Conclusion: These preliminary data strongly indicate that ERC-1671 could be effective in the treatment of progressive malignant gliomas. On the basis of these preliminary data, we are planning a larger study to assess the efficacy of ERC-1671 in the treatment of patients with recurrent GBM.
机译:目的:多形性胶质母细胞瘤(GBM)是一种高度侵袭性的肿瘤,尽管切除,聚焦束放射和替莫唑胺化学疗法均可复发。复发时,美国食品和药物管理局批准的唯一二线治疗药物是贝伐单抗(Avastin)。迄今为止,在贝伐单抗治疗失败后,尚无单一药物能延长进行性恶性神经胶质瘤患者的寿命。一旦在贝伐单抗治疗期间肿瘤复发,就普遍致命,几周内死亡。 ERC-1671是一种实验性治疗策略,它使用患者自身的免疫系统攻击肿瘤细胞。我们报告了单人,有同情心的使用协议下对患有渐进性,贝伐单抗耐药的GBM患者的首次人类ERC-1671疫苗接种的初步数据。方法:治疗涉及对GBM肿瘤细胞患者进行顺序给药然后将来自三个不同供体的细胞裂解液与GBM混合,然后是患者自己的肿瘤细胞和裂解液。结果:患者在接种疫苗后存活了十个月,没有任何其他辅助治疗,并死于与先前化疗相关的并发症。在两个疫苗接种周期后和死亡时收集的组织显示出强大的免疫反应,没有存活的肿瘤。结论:这些初步数据强烈表明ERC-1671可以有效治疗进行性恶性神经胶质瘤。基于这些初步数据,我们正计划进行一项更大的研究,以评估ERC-1671在复发性GBM患者治疗中的疗效。

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